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Items: 1 to 20 of 504

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125069insertion1nstd186human GRCh37 chrX: 2,991,571-2,991,571 , GRCh38.p12 chrX: 3,073,530-3,073,530 ARSF
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979470copy number variation1nstd209human GRCh38 chrX: 3,093,681-3,109,071 , GRCh37.p13 chrX: 3,011,722-3,027,112 ARSF
    nsv5978299copy number variation1nstd209human GRCh38 chrX: 3,082,125-3,090,818 , GRCh37.p13 chrX: 3,000,166-3,008,859 ARSF
    nsv5956393insertion1nstd209human GRCh38 chrX: 3,073,531-3,073,531 , GRCh37.p13 chrX: 2,991,572-2,991,572 ARSF
    nsv5874040copy number variation1nstd209human GRCh38 chrX: 3,112,535-3,112,584 , GRCh37.p13 chrX: 3,030,576-3,030,625 ARSF
    nsv5726241mobile element insertion1nstd211human GRCh38 chrX: 3,102,218-3,102,218 , GRCh37.p13 chrX: 3,020,259-3,020,259 ARSF
    nsv5623929insertion1nstd207human GRCh38 chrX: 3,073,680-3,073,680 , GRCh37.p13 chrX: 2,991,721-2,991,721 ARSF
    nsv5612329insertion1nstd207human GRCh38 chrX: 3,073,533-3,073,533 , GRCh37.p13 chrX: 2,991,574-2,991,574 ARSF
    nsv5612244insertion1nstd207human GRCh38 chrX: 3,112,535-3,112,535 , GRCh37.p13 chrX: 3,030,576-3,030,576 ARSF
    nsv5559823mobile element insertion1nstd206human GRCh38 chrX: 3,102,218-3,102,269 , GRCh37.p13 chrX: 3,020,259-3,020,310 ARSF
    nsv5549102insertion1nstd206human GRCh38 chrX: 3,073,530-3,073,530 , GRCh37.p13 chrX: 2,991,571-2,991,571 ARSF
    nsv5431019copy number variation1nstd206human GRCh38 chrX: 3,077,847-3,078,000 , GRCh37.p13 chrX: 2,995,888-2,996,041 ARSF
    nsv5428791copy number variation1nstd206human GRCh38 chrX: 3,103,499-3,104,713 , GRCh37.p13 chrX: 3,021,540-3,022,754 ARSF
    nsv5416001copy number variation1nstd206human GRCh38 chrX: 3,092,941-3,102,786 , GRCh37.p13 chrX: 3,010,982-3,020,827 ARSF
    nsv5413992copy number variation1nstd206human GRCh38 chrX: 3,095,811-3,097,298 , GRCh37.p13 chrX: 3,013,852-3,015,339 ARSF
    nsv5366346translocation1nstd200human GRCh38 chrX: 3,092,953-3,092,953 , GRCh38 chrX: 3,093,007-3,093,007 , GRCh37.p13 chrX: 3,010,994-3,010,994 , GRCh37.p13 chrX: 3,011,048-3,011,048 ARSF
    nsv5191305mobile element insertion1nstd203human GRCh38 chrX: 3,102,203-3,102,218 , GRCh37.p13 chrX: 3,020,244-3,020,259 ARSF
    nsv5184704mobile element insertion1nstd203human GRCh38 chrX: 3,080,259-3,080,305 , GRCh37.p13 chrX: 2,998,300-2,998,346 ARSF
    nsv5184467mobile element insertion1nstd203human GRCh38 chrX: 3,093,017-3,093,025 , GRCh37.p13 chrX: 3,011,058-3,011,066 ARSF
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